## Abstract A simple, selective and rapid analytical method for determination of trimethoprim (TMP) in honey samples was developed and validated. This method is based on a SPE technique followed by HPLC with photodiode array detection. After dilution and filtration, aliquots of 500 μL honey samples
Rapid method for the determination of eight chlorophenoxy acid residues in environmental water samples using off-line solid-phase extraction and on-line selective precolumn switching
✍ Scribed by J.V. Sancho-Llopis; F. Hernández-Hernández; E.A. Hogendoorn; P. van Zoonen
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 544 KB
- Volume
- 283
- Category
- Article
- ISSN
- 0003-2670
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✦ Synopsis
Gctadecyl (C,,) bonded porous silica sorbent cartridges and Empore membrane extraction discs were evaluated for the solid-phase extraction (SPE) of organochlorine (lindane, dicofol, chlorfenson and tetradifon) and organophosphorus pesticides (dimethoate, fenitrothion and methidathion) from ground water. The SOO-mg Cts cartridges quantitatively adsorbed these pesticides, including the most polar (dimethoate), with recoveries ranging from 68 to 113% for a ground water sample spiked at the 0.1 pg I-' level. SPE with 500-mg C,, Empore discs also quantitatively adsorbed the pesticides with recoveries between 73 and 115% for the 0.1 pg I-' level, but only after eluting with 15 ml of ethyl acetate compared with 4 ml using cartridges and a longer analysis time per sample. After elution with ethyl acetate, the extract was concentrated to an appropriate volume, between 100 and 500 ~1, under a gentle stream of nitrogen. Detection limits were lower than 0.1 pg l-', which is currently the mazimum level allowed by the EEC for pesticide residues in drinking water. Determination was effected by capillary gas chromatography using electron-capture and nitrogen-phosphorus detectors.
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